(Q35748057)

English

Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hürthle cell tumors

scientific article published on May 2002

In more languages

default values for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hürthle cell tumors (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

mitochondrial DNA

0 references

author name string

Valdemar Máximo

1

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Paula Soares

2

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Jorge Lima

3

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

José Cameselle-Teijeiro

4

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Manuel Sobrinho-Simões

5

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

language of work or name

0 references

publication date

1 May 2002

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

The American Journal of Pathology

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

160

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

1857-1865

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Hürthle cell tumours of the thyroid. A review with emphasis on mitochondrial abnormalities with clinical relevance

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Maintenance and integrity of the mitochondrial genome: a plethora of nuclear genes in the budding yeast

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Facile detection of mitochondrial DNA mutations in tumors and bodily fluids

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Suppression of a mitochondrial tRNA gene mutation phenotype associated with changes in the nuclear background

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Solitary, multiple, and familial oxyphil tumours of the thyroid gland

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Microsatellite instability in thyroid tumours and tumour-like lesions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

A gene predisposing to familial thyroid tumors with cell oxyphilia maps to chromosome 19p13.2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Somatic mutations of the mitochondrial genome in human colorectal tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Microsatellite instability in the mitochondrial DNA of colorectal carcinomas: evidence for mismatch repair systems in mitochondrial genome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

The unusual structures of the hot-regions flanking large-scale deletions in human mitochondrial DNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Microsatellite instability, mismatch repair deficiency, and genetic defects in human cancer cell lines.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Oxidants, antioxidants, and the degenerative diseases of aging

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Hypermutability and mismatch repair deficiency in RER+ tumor cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Different cellular backgrounds confer a marked advantage to either mutant or wild-type mitochondrial genomes.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Complementation and segregation behavior of disease-causing mitochondrial DNA mutations in cellular model systems

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Somatic mitochondrial mutation in gastric cancer

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Covalent binding of polycyclic aromatic compounds to mitochondrial and nuclear DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Oncocytic transformation of choroid plexus epithelium

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Mitochondrial myopathies. Clinical, morphological and biochemical aspects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Involvement of choroid plexus in mitochondrial encephalomyopathy (MELAS).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Oxidative damage to DNA: relation to species metabolic rate and life span

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Assembly of functional proton-translocating ATPase complex in yeast mitochondria with cytoplasmically synthesized subunit 8, a polypeptide normally encoded within the organelle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Marked replicative advantage of human mtDNA carrying a point mutation that causes the MELAS encephalomyopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Characterization of insertion mutations in the Saccharomyces cerevisiae MSH1 and MSH2 genes: evidence for separate mitochondrial and nuclear functions

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Role of superoxide dismutase in cancer: a review

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Localization on Mitochondrial DNA of Mutations Leading to a Loss of Rutamycin-Sensitive Adenosine Triphosphatase

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

12 July 2018

Defective mitochondrial ATP synthesis in oxyphilic thyroid tumors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

High frequency of homoplasmic mitochondrial DNA mutations in human tumors can be explained without selection

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Detection of mitochondrial DNA mutations in pancreatic cancer offers a "mass"-ive advantage over detection of nuclear DNA mutations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Somatic mitochondrial DNA (mtDNA) mutations in papillary thyroid carcinomas and differential mtDNA sequence variants in cases with thyroid tumours

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Mutations in mitochondrial control region DNA in gastric tumours of Japanese patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Prevalence of minisatellite and microsatellite instability in radiation-induced post-Chernobyl pediatric thyroid carcinomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Absence of electron transport (Rho 0 state) restores growth of a manganese-superoxide dismutase-deficient Saccharomyces cerevisiae in hyperoxia. Evidence for electron transport as a major source of superoxide generation in vivo.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Mitochondrial DNA is a major cellular target for a dihydrodiol-epoxide derivative of benzo[a]pyrene.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Identification of a mononucleotide repeat as a major target for mitochondrial DNA alterations in human tumors

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Tissue-specific selection for different mtDNA genotypes in heteroplasmic mice

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1850872

25 September 2018

Hashimoto thyroiditis is associated with defects of cytochrome-c oxidase in oxyphil Askanazy cells and with the common deletion (4,977) of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Fidelity of mammalian DNA polymerases

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Microsatellite instability and mutation of mitochondrial and nuclear DNA in gastric carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Comments on: Mutations in Mitochondrial Control Region DNA in Gastric Tumours of Japanese Patients, Tamura, et al. Eur J Cancer 1999, 35, 316–319

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Microsatellite instability, mitochondrial DNA large deletions, and mitochondrial DNA mutations in gastric carcinoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

The common deletion of mitochondrial DNA is found in goiters and thyroid tumors with and without oxyphil cell change

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Mitochondrial gene mutation, but not large-scale deletion, is a feature of colorectal carcinomas with mitochondrial microsatellite instability

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Mitochondrial DNA 'common' deletion in Hürthle cell lesions of the thyroid

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Detection of damage to the mitochondrial genome in the oncocytic cells of Warthin's tumour

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Analysis of nuclear and mitochondrial DNA alterations in thyroid and renal oncocytic tumors

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Functional and molecular analysis of mitochondria in thyroid oncocytoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Coordinate expression of nuclear and mitochondrial genes involved in energy production in carcinoma and oncocytoma

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Mitochondrial Diseases and Myopathies: A Series of Muscle Biopsy Specimens with Ultrastructural Changes in the Mitochondria

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Kearns-sayre syndrome: oncocytic transformation of choroid plexus epithelium

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Absence of microsatellite instability in thyroid carcinomas

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Benign and malignant thyroid lesions show instability at microsatellite loci

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9440%2810%2961132-7

7 January 2021

Nuclear and mitochondrial genome instability in human breast cancer

1 reference

https://pubmed.ncbi.nlm.nih.gov/12000737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The frequency of 4977 base pair deletion of mitochondrial DNA in various types of liver disease and in normal liver

1 reference

https://pubmed.ncbi.nlm.nih.gov/12000737

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1016/S0002-9440(10)61132-7

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 August 2017

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q35748057&oldid=1585117908"